FDA label f18f66cd-ecbf-4aa3-9c74-3957ad847157

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID
4d8aeba0-4848-4093-a723-1db50301d025
SPL ID
f18f66cd-ecbf-4aa3-9c74-3957ad847157
Version
2
Effective date
2019-12-30
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:13:08

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

​Warnings For vaginal use only Not for oral consumption Not for treatment of sexually transmitted infection Ask a doctor before use if pregnant or nursing Ask a doctor before use if you have vaginal bleeding, sores, ulcerations, fever, chills, sensitivity or pain in your lower abdomen or pelvis, a sexually transmitted infection, or suspect a sexually transmitted infection, or pelvic inflammatory disease. ​Stop use and ask a doctor ​if symptoms persist or worsen, or if you have a burning sensation or itching becomes worse. Avoid sexual intercourse when using this product. Using latex condoms during a course of treatment is not reccommended as it is unknown whether this product degrades the quality of a condom. Not to be used as a contraceptive or to treat sexually transmitted infections. ​KEEP OUT OF REACH OF CHILDREN ​If swallowed get medical assistance and contact a Poison Control Center (1-800-222-1222) immediately. KEEP OUT OF REACH OF CHILDREN If swallowed get medical assistance and contact a Poison Control Center (1-800-222-1222) immediately.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.